Nonwoven Pad

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K980720 ↗

FDA Product Code

KMF

Device Class

Class I

Regulation

21 CFR Part 880.5090

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Duoderm(R) Adhesive Compression Bandage, Modified

  Class I

  FDA 510(k) K912550 Active Cleared 14 Aug 1991

• Duoderm Dressings, Cgf Dressings, Paste Full Thick

  Unclassified

  FDA 510(k) K904852 Active Cleared 25 Jan 1991

• Stomahesive Skin Barrier Sterile

  Class I

  FDA 510(k) K851840 Active Cleared 24 Jun 1985

• Allkare Barrier Wipe

  Class I

  FDA 510(k) K925004 Active Cleared 12 Jan 1994

• Duoderm* Extra Thin Flexible Hydrocolloid Dressing

  Class I

  FDA 510(k) K891696 Active Cleared 4 May 1989

• Free & Active(Tm) Absorbent Pads

  Class I

  FDA 510(k) K862878 Active Cleared 19 Nov 1986

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